Guardian Drug Co. Inc. recalls Goodsense Ultra Strength antacid tablets due to small metallic particles in chewable tablets. Consumers should check product details and contact the company for remedy.
Presence of foreign substance: small metallic particles in chewable tablets.
Guardian Drug Co. Inc. is recalling Goodsense Ultra Strength antacid tablets because they contain small metallic particles. This could cause injury if swallowed, so affected consumers should stop using the product and contact the company for instructions.
The tablets contain small metallic particles that could be swallowed and cause injury. This is a foreign substance hazard that might lead to internal damage if ingested.
People who own or use Goodsense Ultra Strength antacid tablets with the specific lot number (1716089) and expiration date (January 2029) are affected. Those who have taken the tablets recently are at higher risk of injury.
Check for the product name 'Goodsense Ultra Strength Antacid Tablets', the lot number 1716089, and expiration date January 2029. The product was distributed by Geiss, Destin & Dunn, Inc. in Peachtree City, GA.
Look for the lot number 1716089 and expiration date January 2029 on the packaging.
If you have the recalled product, stop using it immediately to avoid potential injury.
No, the product contains small metallic particles that could cause injury if swallowed. Do not use the product.
Check the lot number 1716089 and expiration date January 2029 on the packaging. The product was distributed by Geiss, Destin & Dunn, Inc. in Peachtree City, GA.
Stop using the product immediately and contact Guardian Drug Co. Inc. for further instructions.
We’ve drafted a message you can send Guardian Drug to request your refund or repair — edit it as you like.
Subject: Recall D-0575-2026 — Guardian Drug Guardian Drug Hello, I own a Guardian Drug that is covered by recall D-0575-2026 from Guardian Drug. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
